List of Genetic Disorders 2

• Adrenoleukodystrophy •
• Amyotrophic Lateral Sclerosis •
• Becker Muscular Dystrophy •
• Beta Thalassemia •
• Central Core Disease •
• Centronuclear (Myotubular) Myopathy •
• Cerebellar Ataxia •
• Charcot-Marie-Tooth Disease •
• Chondrodysplasia Punctata •
• Congenital Aganglionic Megacolon •
• Conradi-Hunnerman Syndrome •
• Cystic Fibrosis •
• Duchenne Muscular Dystrophy •
• Factor VIII Deficiency •
• Factor IX Deficiency •
• Familial Spastic Paraparesis •
• Fragile X Syndrome •
• Friedrich's Ataxia •
• Gardener Syndrome •
• Glycogen Storage Disease •
• Happle Syndrome •
• Hemophilia •
• Hereditary Motor-Sensory Neuropathy •
• Hereditary Spastic Paraplegia •
• Hers Disease •
• Hirschsprung Disease •
• Huntington's Disease •
• Hypoxanthine-GuaninePhosphoribosyl Transferase (HPRT) Deficiency •

• Ichthyosis •
• Ichthyosis Follicularis, Atrichia and Photophobia Syndrome •
• Ichthyosis, Hepatosplenomegaly, and Cerebellar Degeneration •
• Ichthyosis, Follicular Atrophoderma Hypotrichosis •
• Ichthyosis, Follicular Atrophoderma Hypohidrosis •
• Kallman Syndrome •
• Kelley-Seegmiller Syndrome •
• Kennedy Disease •
• Lesch-Nyhan Syndrome •
• Lou Gehrig's Disease •
• Mitochondrial Myopathy •
• Myopathies •
• Myotonia Congenita •
• Myotubular Myopathy •
• Nemaline Myopathy •
• Nephrolithiasis •
• Paramyotonia Congenita •
• Parkinson's Disease •
• Periodic Paralysis •
• Peroneal Muscle Atrophy •
• Polycystic Ovary Syndrome •
• Prostate Cancer •
• Retinitis Pigmentosa •
• Sickle Cell Anemia •
• Spinal and Bulbar Muscular Atrophy •
• Stein-Leventhal Syndrome •
• Strumpell Disease •
• Tay-Sachs Disease •
• Thrombocytopenia •
• Von Willebrand Disease •

list provided by: http://www.tylermedicalclinic.com/diseases.html